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By G. Dodbiba, T. Fujita, M. Kawata, S. Yamasaki, K. Mitsuhashi, J. Ponou, Y. Iwazaki, T. Atarashi

"The grade of copper ore and concentrate is recently decreasing and it will continues decrease further in the future. The effective liberation treatment for low grade copper ore and the removal of arsenic from copper concentrate is becoming even more important. In this work, the magnetic separation of copper concentrate by heat treatment and the flotation of low grade copper ore by microwave irradiation was studied. The heat treatment of copper minerals in the air atmosphere, the magnetization of most copper minerals increases and especially the magnetization of chalcopyrite shows the largest magnetization, after being heated at 500 oC. The wet HGMS of copper concentrate has been studied and the results have then been compared with the ones when calcined concentrate was used instead. The microwave treatment before ball milling increased the degree of liberation up to 100%, especially when compared with the case when only ball mill was applied to the as-received ore. The flotation of ground copper ore after microwave irradiation showed that the grade copper minerals such as chalcosite and bornite in froth part is much larger than that of tailing part.INTRODUCTION The copper has been used many kind of technological fields and will be more important for the future technology. The global copper production from mine is predicted as shown in Figure 1 (Northey, S. 2014). The copper production peak will be appeared in 2030 and the demand peaks in 2040. In the future the recycling of stocked copper and copper alloy will be necessary to satisfy the demand (Yoshimura, A. 2018). Changes in the grade of copper in copper concentrate, exported from several countries are shown in Figure 2. The copper grade in copper concentrate after mineral processing is gradually decreases every year and it is less than 30% nowadays. On the other hand, the copper ore grade change and prediction are shown in Figure 3. The grade of copper ore is also decreasing to less than 1% in 2010 (Northey, S. 2014). In the future the copper grade gradually decreases, reaching to less than 0.5% in 2080 and the energy to produce the copper metal will increase. The effective liberation treatment for low grade copper ore and the removal of arsenic from copper minerals become more important, nowadays. The microwave irradiation of copper ore for the liberation, energy etc. has been reported by several researchers (for example, Batchelor, A.R. 2017). The magnetization change of copper ore by heating has been reported to remove the arsenic (Sawada, M 2015). In this report, the magnetic separation of copper concentrate by heat treatment and the flotation of copper concentrate by microwave irradiation are discussed after the characteristics of secondary copper minerals are investigated by these treatments."

Jan 1, 2018

"A sulfide ore containing 2.19 g/t Au and 13.13 g/t Ag was studied for the deportment and extractive metallurgy of pay metals. The ore is composed mainly of non-sulfide minerals with approximately 10% pyrite and minor amounts of marcasite, chalcopyrite, galena, sphalerite, and arsenopyrite. The deportment study using a comprehensive approach showed that gold and silver minerals in the ore are mainly native gold (Au), electrum (Ag, Au), petzite (Ag3AuTe2), hessite (Ag2Te) and volynskite (AgBiTe2) with minor amounts of acanthite (Ag2S) and argyrodite (Ag8GeS6). At current grinding fineness (P70@150µm), the majority of liberated native gold and electrum particles are larger than 20µm with 85% >40µm, some of them are even larger than 150µm, indicating that extended leach time may be required to dissolve these coarse gold grains to completion and gravity concentration needs to be considered. Petzite is relatively fine with all liberated particles being less than 80µm in size. Gold distribution and leach testwork results showed that liberated gold accounts for 50% of the head assay, exposed gold associated with sulfide and non-sulfide minerals accounts for 30% and 11% of the head assay, respectively. Gold locked in sulfide and non-sulfide accounts for 4.8% and 4.1%, respectively. Thus, it is recommended that cyanide leaching be considered for extracting gold in this ore. This paper presents the detailed results of the gold and silver deportment study and extractive metallurgy testwork, and discusses the impact on process selection and flowsheet development.INTRODUCTION Gold and silver have been found in various geological environments and ore types. In terms of the gold deportment and extractability, gold ores can be classified into two categories and 12 types. Their extractive metallurgy is largely driven by mineralogical factors such as particle size, association with other minerals, coatings and rimmings, presence of cyanicides, oxygen consumers and preg-robbers, presence of refractory gold minerals and locking of submicroscopic gold in sulfide and sulfarsenide mineral structures (Zhou et al., 2004; Marsden & House, 2006; Zhou, 2013a, 2013b). Compared to gold, silver mineralogy is more complex and metal extraction is more challenging due to its presence in over 200 Ag-bearing minerals (a silver-rich ore body would typically contain 5 to 10 different silver minerals) (Gasparrini, 1984), presence of refractory silver minerals (such as pyrargyrite, prustite and stephanite) and submicroscopic silver in sulphide minerals (such as galena and copper minerals) (Chryssoulis et al., 1985; Di Prisco et al., 2002). The presence of these issues often causes problems in Ag-bearing ore processing. Therefore, knowing the deportment of gold and silver in the ores and metallurgical products is important for flowsheet development and process optimization."

Jan 1, 2018

By V. A. Chanturiya

The results study the minerals oxidation were obtained by us during the methods of microscopic, FT-IR spectroscopic, XRD and chemical analyses of sulphides in tailings of copper-nickel wastes in Kola peninsula. Sulphide minerals begin to oxidize already at the stage of stockpiling and initial stages of storing. The proportion of non-ferrous metals and magnesium oxide increases with time, calcium partially precipitating in the form of gypsum. Comparison of heavy metal contents in pore solutions in cur-rent and stale copper-nickel ore concentration tailings has revealed a significant difference in practically all the parameters. The lower metal contents in current tailing pore solutions (by 5~30 times) are probably due to the presence of float reagent residues blocking oxidation. Much lower concentrations of magnesium and calcium can be accounted for by the difference in kinetics: the rate of sulphide oxidation at this stage is much higher than that of solution interaction with non-metallic minerals as the result of which the solid phase ? solution equilibrium is not achieved. It is generally believed worldwide that it the mining wastes with acidic pore solutions that pose the greatest hazard for the environment. Our findings suggest that although the solution pH in all the samples is higher than 7.8, the contain heavy metal concentrations by far exceeding permissible values. The direct determination of the total and silicate Ni contents in the tailings from current production and in storage tailings has shown that both sulphide and silicate Ni forms occur in tailings. However, the role of silicate Ni is much larger in the storage tailings. The average silicate Ni content accounts for 10% of the bulk Ni content in the current tailings and it increases to 40% in the storage tailings. Thus, the storage tailings are marked not only by sulphide oxidation and the removal of water-soluble sulfates, but also by the interaction of sulfates with the silicate matrix. Although complete equilibrium is not achieved even within 30 yr under polar-region conditions, the major part of the Ni in fine-grained fractions passes into silicate form. The probability of Ni transition to the silicate form directly correlates with the dispersion of the material and the amount of chemically reactive serpentine and hydrochlorite. The migration of Ni as sulfates and its precipitation by chemically active silicates distorts the distribution of this component in the coarse- and fine-grained fractions that are typical of tailings from the current production of copper-nickel ores. On the one hand, the variation of the mode of Ni occurrence in storage tailings lowers the value of technogenic raw materials as a source of this metal.

Jan 1, 2014

By S. M. H. Haddad, M. Saghaeian, R. Hejazi

"Due to limited water resources in mineral processing plants, increasing the efficiency of iron tailing dewatering system in order to obtain more usable water is very important. In this research, flocculation process, as one of the best method for water recovery, was investigated by using one organic cationic and three anionic types of flocculants with different dosages (10, 20, 30 g/ton) and iron ore tailing slurry (8 % w/w solidity) in series of graduated cylinders and obtained results were compared. it is observed that for tailing sample, the anionic flocculants have a significant effect on the settling rate of solid particles compared to the cationic types. Furthermore, effects of temperature (10, 23 and 43 ºC) and pH (2, 7 and 12) on the rate of settlement and turbidity was studied by utilizing the best flocculant. Findings showed that by increasing the amount of flocculant dosage, sedimentation rate went up and turbidity decreased. Comparison the out-put data of tests indicated that at temperature 23 °C and pH=7, the best results for both of faster settling rate and producing more clear water were reached. It should be considered that lower temperature has a more negative effect on the sedimentation rate and overflow water quality. So it will be predicted that for cold seasons, the consumption of the flocculant powder would be higher than the moderate or warm seasons. Also, coagulation/flocculation was evaluated by applying organic cationic coagulant added to anionic flocculant in three different times. Different ratios of coagulant to flocculant was examined (70%:30%, 50%:50%, 30%:70%) as well. Overall, utilizing coagulant had desirable influence on sedimentation experiments and obtaining high quality water. 1- INTRODUCTION In mineral Factories, among the important processes, solid-liquid separation process due to limited resources of water is very important and operates on iron ore tailing in settling tank as thickener in order to gain clear water for preventing water loss and applying again in plant units (Ciftci and Serhat Isik, 2017). Iron ore tailing include inharmonious compounds of iron oxides, silicates and aluminum-silicates. The percentage of solid in the tailing usually changes between 5 and 10 percent (Dash et al., 2011). One of the major problem about dewatering of tailing in thickener is solid-liquid separation of slurries with high stability because of fine particles. It means that rate of sedimentation is very slow and recovered water quality is inappropriate. This issue can be solved to a large extent by factors such as pH control, ionic strength and flocculation/coagulation process which results in aggregation of particles so that settlement by gravity is happened (Dash et al., 2011)."

Jan 1, 2018

By ?. S. Potokin

"In general the electric pulse treatment is composed from two processes – electric pulse grinding and electric explosive (electric discharging) activation. The electric pulse grinding with the effect of selective destruction refers to a major slag fraction, more that 2-5 mm, when a one can see a physical prerequisites for electrical breakdown of the slag particles. The electric pulse treatment of slag is considered as an additional operation in the technological scheme extraction of non-ferrous metals from copper smelting slags in addition with mechanical grinding, flotation enrichment and acid leaching. Studies of the reprocessability of pelletized slag have shown the possibility of higher extracting non-ferrous metals via flotation after electric pulse disintegration (EPD) treatment. By using EPD of slag pellets, it is possible to increase the non-ferrous metal yield to concentrate by 18-24%.INTRODUCTION The use of the explosive effect of the plasma discharge channel at electrical breakdown of a solid at a pulsed high voltage is the physical basis of the electric pulse method of destruction of geomaterials (Vorobiev et al., 1971; Andres, 1995; Semkin et al., 1995). The flowing of a pulsed current in the discharge channel is accompanied by a sharp increasing of plasma’s temperature and pressure, leading to a supersonic expanding of the discharge channel, the formation in the solid of intensive mechanical tension field, spreading of cracks, and eventually, to the destruction of the solid. Fragmentation and grinding of ore and mineral aggregates by electric pulse method due to a number of specific physical mechanisms of power load and crack formation, belonging only to this method, is different by high selectivity of destruction. This ensures better liberation of grains of individual minerals and their better preservation from destruction and less formation of a slurry output. These features creates the prerequisites for a more complete extraction of a useful mineral in the concentrate during ore dressing, to improve the quality of concentrate. In contradistinction to mechanical methods, electric pulse technology does not contaminate the product with instrumental metal, material of lining and grinding bodies. The possibility simply and in a wide range to change the dynamic load character allows to regulate the granulometric composition of the product of grinding, to obtain a narrower class of product size than is possible with mechanical grinding. The product of electric pulse grinding is characterized by less roundness and large specific surface area of grains due to the trait, that a new surface is formed in the process of splitting during the expanding of cracks. The degradation product has increased sorption and reactivity in chemical reactions. Liberation of the mineral inclusions particle better corresponds to their initial natural state in the rock and this is the great importance for the study of mineral raw materials."

Jan 1, 2018

By L. A. Vaisberg, E. V. Shishkin, S. V. Kazakov

"This research is targeted at finding solution to the problem of reduction of specific energy consumption during disintegration of solid materials with the help of machines, operating in a quasiresonant mode. The objective of the research is the development of an energy-saving method of disintegration of supestrong rock and by-products on the basis of vibrational units with two movable crushing elements, operating in a rigorous synchronous-antiphase mode without stringent kinematic links. In the course of investigations a mathematical analysis of the dynamics of vibrational units was performed to determine required mechanical parameters, allowing for adjustment of the machine actuating elements to high-frequency synchronous-antiphase oscillations in the quasiresonant frequency range. As a result of performed pilot tests, the reliability of desktop studies was confirmed and the dependency of process parameters on the machine regulated parameters in the quasiresonant frequency range was identified. The analysis of obtained data showed that during machine operation with cone-shaped crushing elements in the quasiresonant frequency range, the yield of the high-quality finished product (WFA grits of -3+1 mm grain size class) in one pass reaches 35%, whereas the form of the particles corresponds to the grain form with sharp edge. The quasiresonant operation mode of the vibrational unit with two freely suspended crushing elements (without stringent kinematic links) provided substantial reduction of energy intensity during crushing down to 0.16 kWh/t, which shows reduction of power consumption for crushing by more than 15% compared to conventional equipment.INTRODUCTION The most common and energy-consuming processes in the mining industry are the crushing and grinding of various solid materials. Such large energy costs are due to the fact that the capabilities of the existing crushing and grinding machines are based on traditional methods of destruction, and are limited by their kinematic features, which do not allow to reduce the energy intensity of processes, to lower the irreversible loss of useful components, to improve the quality of marketable products. In connection with the foregoing, the task of energy costs reducing for disintegration is one of the most important issues in the enrichment of both minerals and processing of man-made raw materials. The solution of this problem is possible only through the creation of a fundamentally new highly efficient technique and technology for processing raw materials [1, 2]. It seems that the greatest prospects in this respect are the vibration methods of disintegration, in particular, the vibratory cone crusher based on a two-mass system without rigid kinematic connections between the crushing bodies, with vertical vibrations of the working bodies. In this machine, the principle of rational material destruction is realized – crushing without re-grinding [3-5]."

Jan 1, 2018

By Kazutoshi Haga, Atsushi Shibayama, Altansukh Batnasan

"The aim of this study was to develop a hydromellurgical processing for removal of arsenic from high-arsenic copper sulfide ores and concentrates, providing increase in copper recovery. In this study, three different enargite ore samples containing 28.2–46.7% copper, 1.9–15.0% arsenic and 10.6–27.5% iron were used to determine optimum conditions for the extraction of copper and removal of arsenic. High pressure oxidative leaching process was preformed using various leaching reagents such as sulfuric acid (H2SO4), ferric sulfate (Fe2(SO4)3), hydrochloric acid (HCl), ferric chloride (FeCl3), sodium sulfate (Na2SO4), sodium chloride (NaCl) solutions and distilled water (DW), respectively, under the fixed conditions which were selected to be as follows: NaCl concentration, 0.34 M; concentrations of other leaching reagents, 0.1 M; particle size, -45 ?m; pulp density, 100 g/L; agitation speed, 750 rpm; leaching temperature, 160 ?C; leaching time, 60 min and total pressure (oxygen gas and vapor pressure) into an autoclave, 1 MPa. Results show that under the leaching conditions, more than 90% of copper leaching was achieved with lower than 2% arsenic content as a consequence of the formation of arsenic precipitates in a solution of Fe2(SO4)3–NaCl. It was determined that copper, arsenic and iron concentrations in the pregnant leach solution were 42 g/L, 0.3 g/L and 0.3 g/L, respectively. As a result, it can be concluded that the Fe2(SO4)3 solution in the presence of NaCl or FeCl3 are more efficient leaching media compared to other leaching agents under the high pressure oxidation conditions, because of their high copper recovery and lower arsenic level in the pregnant leach solution.INTRODUCTION Generally, copper is usually produced from copper sulfide ores by a combination of several processes which are flotation and smelting followed by refining [1-3]. Arsenic content in copper sulfide ores tends to increase due to the depletion of high grade copper deposits, hence conventional mineral processing and metallurgical processes cannot effectively treat these ores containing high levels of arsenic to obtain consistently high purity copper concentrates. Because high levels of arsenic in copper ores/flotation concentrates reduces the value of concentrates due to the restriction of smelting process and causes it to be a source of environmental pollution [4-6]. From this point of view, the known way of prevention against high-arsenic copper sulfide concentrates in further metallurgical treatments is to develop economically and environmentally competitive technologies for removal of arsenic impurity from copper sulfide ores before treating the ores/flotation concentrates by the pyrometallurgical routes."

Jan 1, 2018

It is well known that the crushing and grinding steps in the mineral processing of ores represent a substantial proportion of total energy, cost and carbon emission in mining. For instance a recent study calculated that 36% of the energy consumed by gold and copper producing mines in Australia was attributable to comminution (Ballantyne et al, 2012). Understanding this component of a business is essential in a world seeking to lower production costs, improve earnings and reduce its carbon footprint. The issue commands the attention and support of industry leaders in the mining sector, government, equipment manufacture, engineering design and research organizations. Furthermore, several researchers have often stated that globally, comminution processes consume between 3-4% of the world?s electrical energy production (Daniel and Lewis-Gray, 2011). In 2009-10, Australia?s Federal Government Energy Efficiency Opportunity (EEO) participants in the mining sector used 336.5 PJ, representing approximately 6 percent of Australia's total energy use. It is evident that the current practices of breaking rocks in tumbling mills are relatively inefficient (Fuerstenau and Abouzeid, 2002). Research and improved engineering design has established that a range of improved blasting, crushing and grinding techniques and flow sheets may lower project costs and carbon footprint. These include relatively simple process flow sheet strategies such as gangue rejection or pre-concentration prior to size reduction, a better combination of grinding technologies (both current and new systems), and selection of coarser grind sizes where ore and waste mineralogy allow. Yet, despite this systematic and detailed research, the industry remains somewhat reluctant to implement these strategies. CEEC (Coalition for Eco-Efficient Comminution) was established in 2011 to support knowledge sharing and change in an area of high-energy consumption for the global mineral industry. CEEC is a not-for-profit industry company, funded by grants from world wide industry companies, whose mission is to accelerate knowledge and technology transfer in the field of energy-efficient comminution. The key benefit to the mining sector arising from CEEC?s activities will be an increase in the rate at which more energy-efficient comminution data sets, processes, and technologies are developed, demonstrated, shared and applied. This will contribute directly to the industry?s target of reducing operating costs and carbon emissions. CEEC International Ltd and JKTech Pty Ltd teamed together to facilitate the inaugural CEEC Workshop, in June 2012. The purpose of the workshop was to produce a roadmap to provide guidelines for how (1) operations can achieve best EEC practice in the short to medium term, in collaboration with vendors, engineering companies and other service providers, and (2) what R&D is needed to achieve paradigm change in EEC in the medium to long term, e.g. 75% reduction in comminution energy in 10 years.

Sep 1, 2012

By S. V. Balikov

A close association of fine gold with pyrite and arsenopyrite is observed at many gold ore deposits. Gold forms and gold distribution in sulfides of different deposits were studied. A comprehensive method including optical spectrum analysis, X-ray diffraction analysis, high-temperature X-ray diffraction analysis, scanning electron microscopy and X-ray microanalysis was used for the de-tailed investigation of the defectiveness of the structure of pyrites from different deposits. It was shown that gold content in pyrites varied from 1.5 g/t to 100 g/t compared with 30 g/t to 230 g/t in arsenopyrites. The nature and arrangement of inner inclusions of foreign minerals in pyrites as well as occurrence of fractures and macro- and microdefects were examined. Iron, sulfur and arsenic contents in all pyrite samples were determined. Chemical composition of the detected inclusions was defined. Parameters of submicroscopic structure of pyrite were estimated using X-ray Fourier line shape analysis. Estimation of real structure characteristics with calculation of submicroscopic D-blocks and root-mean-square lattice deformation 2()evalues was performed. Defectiveness of the pyrite structure can be defined by the following parameters: K?1 and K?2 reflection resolution and its intensity within high Bragg angles; S content to Fe content ratio; the arsenic content and the local variation in its concentration within the pyrite grain; the size of submicroscopic blocks and the crystal lattice disturbance value. The performed analysis showed some relationships between these parameters and refractoriness of the pyrite concentrates. It was observed that at S/Fe ratio close to or higher than stoichiometry and at a low arsenic content (less than one per cent) pyrite concentrates were not refractory. The analysis results showed that concentrates of the Beryozovskaya gold plant (0.02~0.07 As%) and concentrates of the Kommunarovskaya gold plant (less than 0.05 As%) as well as some pyrites from the Sukhoi Log gold deposit had the same characteristics. It was found that average arsenic content did not excess 0.2 per cent. Arsenic distribution within the grain of all these pyrites was uniform. At S/Fe ratio lower than or close to stoichiometry and at high arsenic content (more than one per cent) and significant variation in its distribution within a pyrite grain the pyrite concentrates are refractory. Such pyrites are typical for the Sukhoi Log, the Bakyrchik and the Mardzhanbulak gold deposits. Direct correlation between arsenic and gold contents, in particular, in fine grains of pyrite was observed by many researches. This correlation was explained by impregnation of arsenopyrite which normally contains more gold than arsenic pyrites. The analyses results showed that no arsenopyrite impregnation was found: arsenic distribution within the grain was uniform but its concentration varied greatly. Such pyrite concentrates are more refractory. This paper presents the results of analyses of sulfides to determine the amenability of the associated gold recovery by hydro- and pyrometallurgy.

Jan 1, 2014

By V. Ross

"The Upper Group 2 (UG2) reef in the Bushveld Complex in South Africa hosts an estimated 40% of the world’s Platinum Group Metal (PGM) resources. The processing of this ore via flotation poses two particular challenges: limiting the levels of chromite in the concentrate to reduce downstream smelting problems, and enhancing the recovery of ultrafine (typically -10 micron), liberated PGMs. Conventional ways of suppressing the entrained chromite, such as froth washing, is not effective in PGM operations, which are dominated by mechanical cells. The recovery of fine particles is hampered by low collision efficiencies with air bubbles, as well as oxidised surface layers especially in tailings operations. This paper documents the results of laboratory tests on a run-of-mine PGM UG2 ore, investigating the application of a pneumo-mechanical column (PMC) and its effect on PGM flotation and its selectivity with regard to chromite. A key feature of the device is the stage-wise release of aerated slurry from an agitated downcomer, thus creating conditions where the superficial velocity profiles of air and slurry change axially within the separation zone. This aids segregation of the silicates and chromite-rich fractions in the separation zone, concentrating the latter towards the bottom of the column and minimising its entrainment into the concentrate. Comparison of the performance of the PMC to that of mechanical laboratory cells under equivalent operating conditions showed improved PGM flotation kinetics and recovery. This was accompanied by a decrease in gangue recovery compared to the mechanical cells by more than 40%, thus doubling the final rougher concentrate grade from 50 to 100 g/t. Significantly, whilst the overall Cr2O3 recovery was reduced by more than 60%, the selectivity (PGM recovery vs Cr2O3 grade in the concentrate) was doubled.INTRODUCTIONThe Bushveld complex in the northern part of South Africa hosts the world’s largest reserves of Platinum Group Metals (PGMs), representing approximately 40% of the total PGE. It is characterised by three main PGM bearing reefs, namely Merensky, Upper Group 2 (UG2) and the Platreef. The Merensky and Platreef are dominated by silicates in the form of pyroxenites, and carry economically recoverable amounts of copper and nickel, in the form of chalcopyrite and pentlandite. The UG2 on the other hand is a chromitite ore with chromite as (ideally, FeO.Cr2O3) the most abundant gangue, often constituting more than 70% by mass with a PGM grade of around 4.5 g/t. Other key gangue minerals are pyroxene, feldspar and talc. The PGEs occur in a wide variety of minerals, with platinum and palladium sulphides typically accounting for about half of the total. Base metal sulphides such as chalcopyrite, pentlandite and pyrrhotite occur in only very minor amounts, accounting mostly for less than 0.1% by mass."

Jan 1, 2018

By Chuanyao Sun, Zhenguo Song, Aijun Ren

"Lead-Zinc sulfide ore containing carbon is one of typical refractory resource. Because organic carbon has natural floatability, it has a great negative influence on flotation of lead-zinc sulfide ores. It is difficult to obtain qualified lead concentrate by flotation using conventional reagent system. In order to reduce the influence of organic carbon on lead and zinc flotation, two alternatives, i.e., removal carbon by pre-flotation or adding carbon depressant in lead and zinc flotation, can be adopted. If the flowsheet of removal carbon by pre-flotation is adopted, the lead and zinc recovery which are lost in the carbon tailings is often higher. If conventional carbon depressants are used in lead and zinc flotation, it has a certain depression effect on lead minerals. In the paper, the ore grading 1.49% Pb, 5.73% Zn, and organic carbon 3.14% has been carried out by flotation tests. In the bulk flotation of carbon and lead minerals, Pb concentrate is only about grading 21.00% Pb. In the pre-flotation of organic carbon, it’s hard to remove most of carbon, and the loss of Pb and Zinc recovery is too much in carbon tailings. New carbon depressant BK547 and three conventional carbon depressants including sodium lignosulphonate, Fe-Cr-lignosulfonate, and dextrin, are used in comparative tests of Pb flotation, and results show that BK547 have a good depression on organic carbon, and have almost no effect on Pb flotation. Using BK547 as carbon depressant, cycle test in flowsheet of two-stage Pb and Zn selective flotation and coarse concentrate regrinding have been carried out, and results show that concentrates grading 62.51% Pb and 41.33% Zn are obtained at recoveries of 70.24% Zn and 83.58% Zn.INTRODUCTION Lead and zinc mineral resources are still the main source of lead and zinc metal. For lead-zinc sulphide ore, lead concentrate and zinc concentrate are obtained by flotation. Minerals separation by flotation is a complex process and is dependent, along with other factors, on the relative distribution of hydrophobic (e.g. collector, polysulfide, elemental sulfide) and hydrophilic (e.g. metal hydroxide) species between different particles of the same mineral phase and between mineral phases (Piantadosi & Smart, 2002; Boulton, Fornasiero & Ralston, 2003). Organic carbon has natural floatability and is often associated with lead-zinc sulphide ores. If the content of organic carbon in the ore is more, the flotation index will become worse. The main problem is that the concentrates has too low grade to be qualified grade products for sale. At the same time, the consumption of reagents is more than ordinary ores without organic carbon. In order to solve the influence of organic carbon on the flotation of lead and zinc and other sulphide ores, a lot of research works have been carried out."

Jan 1, 2018

By J-P Franzidis, P. O. Gyebi

"Coal-water mixtures (CWM) of concentrated fine coal may be transported in pipelines but this is influenced by both CWM rheology and stability. Here, a low viscosity is required to reduce power requirements, as well as good stability for transport and storage. The objectives of this study are to investigate the importance of surface charge, solids concentration and dispersant addition on the rheology and stability of a fine Witbank coal-water mixture (<75 m). Zeta potential, rheology and stability were measured with a Malvern Zetasizer, a AR1500EA rheometer and a static rod penetration test, respectively. Sendep 30D, Sendep 30F and Norilose 8058, all supplied by Senmin International, were used as dispersants, at dosages of between 0.1 to 0.5% dry coal (w/w). Solids concentration was varied from 10 to 58% (w/w). The zeta potential was found to be positive at low pH and decreased sharply with increasing pH to a minimum of -50 mV at pH 10. The zeta potential decreased with increasing dispersant concentration for all dispersants. The lowest zeta potential of -63 mV was obtained for Norilose 8058 at a dosage of 0.3%. CWM rheology was Newtonian at lower solids concentrations but became non-Newtonian at solids concentrations over 40% (w/w), with an initial yield stress and pseudo plastic behavior. The yield stress decreased sharply with increasing dispersant concentration for all dispersants. The lowest yield stress was obtained for Norilose 8058. The addition of dispersants resulted in significant improvements in stability. A penetration ratio of over 70% was obtained for Norilose 8058 after 10 days. In summary, the addition of dispersants resulted in a decrease in the zeta potential which increased the electrostatic repulsive forces between particles, thus improving both CWM rheology and static stability.INTRODUCTION Coal Water Mixtures South Africa’s energy economy depends heavily on coal. It accounts for about 70% of primary energy consumption, 93% of electricity generation and 30% of liquid petroleum fuels (Eberhard, 2011). The transportation of coal to export markets and power generation stations is a problem in the South African coal industry due to ageing and inefficient rail infrastructure. This problem is intensified by the long distance of coal haulage, delays in the time required to load and unload wagons, and environmental challenges related to air pollution and water contamination. Fine coal may be transported more efficiently and economically in a pipeline as a highly concentrated coal water mixture (CWM). Typically a fine coal CWM will contain 60-75% coal, 25-40% water and nearly 1% of dispersing additives (Atesok et al., 2005; Dincer et al., 2003). However, the transport of CWMs in pipelines is strongly influenced by both CWM rheology and stability. Here, a low viscosity is required to reduce power requirements, as well as good stability for transport and storage. These quantities are affected by the coal composition/mineralogy, solids concentration, particle size and size distribution, particle shape, inter-particle forces and dispersant type and dosage (Laskowski, 2001)."

Jan 1, 2018

By A. Kurkov

Flotation process is based on the formation of primary collector-based supramolecular associates at the mineral surface and within the pulp. Supra molecular chemistry allows studying within a common framework, all kinds of molecular associates, from dimers to large assemblies, resulting from spontaneous association of a large number of interacting components of the flotation system, where the collective action of non covalent bonds can have an important role. Self-organization of supra molecular assemblies in the flotation process can be controlled by modifying the chemical structure of the collector, the nature and arrangement of functional group in it, by introducing secondary agents (SA) into the process, to adjust the interaction between the collector and the surface and to control the hydrophobicity of the adsorption bed. This offers broad opportunities to build supramolecular assemblies to improve the efficiency of flotation. Besides, the more complex is the system, the weaker are the interactions, that determine its behavior. This powerful factor still is not employed deliberately to control the flotation process. Organophosphorus compounds (OPC) - dialkyl phosphoric acids whose radicals contain ethoxylated groups ? are considered as nanocompounds, that can be used in building supramolecular assemblies. The presence in an OPC molecule of functional groups (P=O, P (O) O-, P (O) OH), ethoxylated groups, and aromatic rings is the basis for the formation of stable supramolecular associates. Gross formula: C54H94KO16P. Molecular weight is 1069.39. Phosphoryl anion has a regular tetrahedral structure with the angle of 109.5°. Lengths of -P-O- bonds in a PN molecule are 1.7345Å; length of the hydrocarbonic radical C42-C72 = 33.942Å. In an alkaline environment, PN is in the form of the anion, in an acidic environment ? in the form of the polycation due to protonation of the oxygen in the EO group. Chem Office software suite was used to generate three-dimensional images of an OPC molecule in acidic and alkaline environments, to reveal the OPC geometry (bond lengths, valence angles, aliphatic radical length), to identify the collector&apos;s binding sites with the mineral surface, to find the most stable and energy-efficient molecular conformations of an OPC molecule and its complexes with minerals under various conditions. Mechanisms of interaction between OPCs and the mineral surfaces are different. In ores whose minerals are dominated by ionic bonds (fluorite), the interaction mainly involves the anionic form of the collector; in ores, whose minerals are dominated by covalent bonds - the oxygen of the phosphoryl group (donor-acceptor interaction) and the oxygen of the ethoxylated groups. This difference is responsible for the formation of spatial associates with different surface layer structures. Introduction of supramolecular chemistry concepts into the analysis of flotation phenomena and mechanisms can become an effective tool for better understanding the flotation process and offers new means of consistently improving its effectiveness.

Sep 1, 2012

By P. V. Ramesh Babu

India has sizeable number of small deposits of rare metal bearing minerals namely columbite-tantalite, pyrochlore, beryl, lepidolite, spodumene and rare-earth element bearing minerals monazite and xenotime in different parts of India. Pegmatites, alkali granites, syenites, and the derived gravel and soils are the main source for rare metal and rare earth (RMRE) minerals. The RMRE minerals are classified as prescribed substances under Atomic Energy act of 1962 keeping in view the uses in the nuclear industry. Atomic Minerals Directorate for Exploration and Research (AMD) of Department of Atomic Energy (DAE) is the sole agency responsible for exploration and exploitation of RMRE minerals in India since 1962. The latest technological advancements and applications in the field of space, electronics, communication and nuclear industry using these metals and their products have necessitated to augment the production and resources of RMRE minerals. These minerals play a significant role in the technological and economic development of the country. The light rare earth element bearing mineral monazite is abundant in beach sands and is being commercially exploited by Indian Rare Earths Limited (IREL). Columbite-tantalite, the chief source for niobium and tantalum (Nb-Ta) metals present in the pegmatitic gravel are recovered by small mobile beneficiation plants. The cut and fill method of mining adapted is eco-friendly. The processing flow-sheet consists of wet sizing at ½ in and 1mm followed by gravity concentration of sized products utilizing the methods of jigging and wet tabling. The sizing equipment include revolving and vibratory screens and the gravity concentration equipments used are fixed sieve jigs and movable screen jigs for final upgradation. The gravity concentrates are further upgraded by magnetic separation to remove magnetite and ilmenite. The mine areas are reclaimed by filling with coarse size tailings and new plantations. These mobile pilot plants were earlier operated in Bihar mica belt, Jharkhand, pegmatitic areas of Karnataka and Nellore mica belt of Andhra Pradesh and are currently being operated in Bastar-Malkangiri pegmatite belt of Chhattisgarh and pegmatites of Jharsuguda district of Orissa. Beryl, lepidolite, spodumene and cassiterite minerals are the by-products from the pegmatite ores. Fergusonite, samarskite and microlite are the other niobium and tantalum bearing minerals which are also found in pegmatites. Xenotime, the chief mineral of yttirium generally occurs in granites and pegmatites. The rare earth minerals monazite and xenotime get concentrated in the placer sands of rivers and beaches. The occurrence of xenotime in the sands of Siri River and Deo River in Chhotanagpur granitic terrain in parts of Chhattisgarh and Jharkhand are an example. These sands containing 1-2.5% heavy minerals were processed by a mobile plant consisting of sizing equipments like trommel and vibratory screen followed by separation of heavy minerals from -1mm sands with the help of gravity concentration equipments like spirals/shaking tables/sluices. Xenotime and monazite from the pre-concentrate are further separated by magnetic and electro-static methods. The present paper illustrates the pilot plant set up for the recovery of rare metal as well as rare earth minerals. Keywords: small deposits, rare earths, rare metals, pegmatite, Nb-Ta, xenotime, India

Sep 1, 2012

By D. J. Borrow, K. van Netten

"A fine coal tailings feed was selectively agglomerated using a concentrated water in oil emulsion binder consisting of 95% aqueous phase and 5% organic phase. The purpose of the study was to investigate a continuous system in plug flow, providing a rapid beneficiation technique with high selectivity and recovery. The development of the novel binder was undertaken in previous work in a batch system consisting of a high-speed blender. In this previous work, it was found that agglomeration could be achieved in 3 s, providing the binder was pre-dispersed. Furthermore, it was found that, depending on the feed, only ~1 wt% of oil was required to achieve agglomeration, some 10 times less than required in traditional oil agglomeration. In a more recent study, the technique was adapted into a continuous process. Due to the rapid speed of the process using the emulsion binder it was found that a simple flow constriction within a 1 inch pipe was sufficient to achieve the selective agglomeration observed in the batch system. In this previous study, a coal feed consisting of a flotation product was agglomerated at a superficial slurry velocity of 1.3 m/s using a partially closed ball valve as the flow constriction. In the current study, a feed consisting of fine coal tailings with an ash content of 50.1% was used to establish the influence of superficial slurry velocity on the agglomeration process. The superficial slurry velocity was varied between 1.3- 4.2 m/s, while maintaining a constant pressure drop of 100 kPa across the flow constriction. The flow constriction consisted of a partially closed ball valve. It was found that increasing the superficial slurry velocity across the flow constriction reduced the amount of organic liquid required to achieve agglomeration. Under the optimum conditions, a combustible recovery of 80.4% was achieved at a product ash content of 9.6%. This work demonstrates a valuable product can be rapidly produced from tailings material using the novel emulsion binder. INTRODUCTION A significant opportunity exists to recover fine coal from material that is currently classified as waste. This waste material, also called tailings, is currently considered not economic to process due to its high ash content, low solids concentration, and the fine size of the particles. Thus, for this opportunity to be realised, a process is required that is highly selective and has the ability to economically recover fine particles at high throughputs. The technique of oil agglomeration has previously been considered as a candidate for the recovery of fine coal, as it is highly selective and has no lower limit on the size of particle that can be recovered (Capes and Jonasson, 1989). However, the cost of the oil required as the binding agent in the process has proven to be a significant barrier to any long-term applications (Swanson, Nicol, and Bensley, 1977). Recently, however, Yoon and co-workers have developed an ultrafine coal separation process that utilizes an oil phase for the recovery of the hydrophobic coal particles and have implemented an oil recycle to greatly reduce the consumption and thus cost of the oil (Yoon et al., 2016)."

Jan 1, 2018

By E. V. Leont'eva, V. R. Vafin, A. G. Kladova, N. L. Medyanik, A. P. Ponomarev

"The thermochemical technology for recovery gold, silver from mature flotation tailings of pyrite ores by two-stage sintering with chlorine-ammonium reagents and leaching of bakes with water is developed. The economic effect of the technology implementation is calculated. KEYWORDS Gold and silver recovery, mature flotation tailings, pyrite ores, chlorine-ammonium reagents, leaching INTRODUCTION The relevance of processing the technogenic reserves of ore mining and concentration wastes accumulated over the long operation periods of mineral deposits is beyond doubt. Hundreds of tons of precious and non-ferrous metals that were not recovered during the primary processing are concentrated in the accumulated wastes. For example, tailing storage facilities (TSF) at the mineral processing plants in the Southern Urals region of Russia hold more than one hundred tons of gold and thousands of tons of silver in the mature flotation tailings (MFT) of copper pyrite ores. Secondary processing of technogenic materials is facilitated by the fact that they are preprocessed — ground and compactly deposited on the surface, but complicated by the low (compared to ores) grade, uneven distribution of the valuable minerals, altered and unstable material composition of the mineral feed. This leads to low recovery rates of valuable metals by conventional physicochemical processing methods. It is necessary to develop innovative methods of deep integrated processing of industrial wastes, based on the study of the material composition of specific technogenic mineral resources and based on ensuring the environmental safety of the resulting secondary waste. MATERIALS AND METHODS The object of this study are the MFT of Uchaly Concentrator in the Republic of Bashkortostan, Russia, which processes copper pyrite and copper-zinc ores. According to the data of particle size, chemical, X-ray phase, and optical microscopic analyzes, samples of the MFT are characterized by considerable particle fineness (the fraction of the size class -41 µm is 89-90%), low grade of gold (1.7-2.0 g/t) and silver (18.0-19.5 g/t), comparable grades of iron (23.0-26.8%) and sulfur (28.1-28.7), but different grades of copper (0.12 - 0.73%) and zinc (0.34-1.26%). The most common mineral in the samples is pyrite (50 - 56%), found in intergrowth with grains of other sulfides (0.1-4%) - sphalerite, tennantite, chalcopyrite, covellite. Quartz and aluminosilicates are the dominant rock minerals (21-36%). Based on the results of the phase analysis, it was established that approximately 70% of the gold in the samples is found in a form that is resistant to cyanidation — it is locked in sulfides (52-56%) and quartz and coated by films. Along with sulfides and rock minerals, common gold and silver minerals (chalcogenides, intermetallides, native gold) in the form of submicro- and nano-sized precipitates are also associated with intergrowth of a complex structure. These features of the material composition allow classifying the MFT of the pyrite ores as a mature feed material and emphasize the need for chemical non-cyanide methods to recover gold and silver from the mature minerals and associations they are found in."

Jan 1, 2018

By Juan B. Yianatos

"After almost 100 years, since the first commercial application began in Australia, flotation has shown an extraordinary growth and nearly 2 billion tons of ore per year are presently treated by flotation processes. During this time flotation has promoted a wide scope of research activities ranging from fundamental chemistry and hydrodynamic studies to studies of industrial operations. In general, fundamental studies have been mainly related to ideal situations. In recent years, however, large efforts have been focusing on achieving a better insight into the actual sub-processes provided by the development of new and more sophisticated instrumentation. Since the massive incorporation of flotation columns, around 15 years ago, a renewed interest in flotation fundamental studies, process modelling and new cell designs have been observed worldwide. The key role of the froth has been recognized as an independent and sometimes rate limiting process step. Thus, separation of pulp and froth process stages seems the most appropriate in terms of process modelling, diagnostic, design and scale-up purposes.In relation to flotation equipment development, until the middle of the 1970?s, only the sub-aeration mechanical cells were dominant. Since the 1980?s, the use of pneumatic cells and forced air mechanical cells has emerged strongly. Also, in the last decade, flotation equipment has shown a dramatic increase in size, reaching values of 200m3 in unitary mechanical cells and more than 300m3 in columns. The general feeling, however, is that, despite the great advance observed in terms of process knowledge, the mechanisms and principles of industrial flotation cells design and scale-up are still not fully understood.Advances in process instrumentation and control now in use allow for more efficient operations, both in metallurgical performance and savings in operating costs.INTRODUCTIONFlotation is a widely used process within the minerals processing industry, as well as being used for water treatment and de-inking of recycled paper. Froth flotation started in Australia at the beginning of the 20th century and since then flotation technology has made significant advances. Flotation was firstly applied to sulfide ores. The largest tonnages treated by flotation are copper and copper/molybdenum ores, handling about 50% of the total ore processed. Also significant are phosphate, iron ore and coal treatments. At present, Chile is the foremost copper producer in the world with around 35% of the world?s production. Figure 1(a) shows the evolution of copper production in Chile over the last decade. The total amount of fine copper produced in year 2001 was 4.7 million tons, from which 3.2 million tons was processed by flotation while 1.5 million tons went through LIX-SX-EW processes, which also showed significant development during the same period (Anon, 2001). The total flotation treatment of copper ores in Chile is about 325 million tons per year (Anon, 2002), so the world treatment of copper ore by flotation can be estimated at about 1 billion tons per year. Consequently a total of nearly 2 billion tons of ore per year is presently processed worldwide by flotation (Fuerstenau, 2001). In order to handle the higher tonnage of low-grade ore, a worldwide trend towards the development and use of larger flotation machines began in the 1960?s. Figure 1(b) shows that the trend became extremely marked from the beginning of the 1990?s, which is consistent with the strong increase in copper production during the same period."

Jan 1, 2003

By Jia Muxin

The adsorption behaviors of metal ions on a silicate mineral and the flotability of a metalized silicate mineral with sodium oleate as collector are closely related to the structure of the silicate mineral. The adsorption isothermals of the metal ions on different silicate minerals are studied, the parameters of the isothermal give the information how many surface oxygen anions a metal ions is attached to, from this information and the structure of the mineral the site where a metal ion is attached can be guessed (The adsorption isothermals and adsorption behaviors with pH are fitted with Temkin, Frenudlich and Kurbatov equations respectively). Metal ions as Cu2+, Ni2+, Zn2+ are attached to the oxygen anions of surface species –Si-O– on the quartz surface, most of them coordinate to only one surface oxygen, their adsorption ability on quartz is low, but this metal ions on quartz surface protrude out of the surface perfectly, so their ability to combine with oleate acid radical is excellent. Quartz can be activated well by such metal ions. The isothermal of Fe3+ on quartz indicates these cations coordinates with more than two surface oxygen anions. This means the Fe3+ nucleates on quartz surface in the form of Fe(OH)3 colloid particles. The isothermals of Cu2+, Ni2+, Zn2+ Fe3+ on spodumene shows such ions coordinate with more than two surface oxygen anions, it indicate these ions may attach to the position where Li+ is formerly exists, such metal ions stay in a cave on the mineral surface, their adsorption abilities on spodumene are quite well, but they are affect by the oxygen anions of the two Si tetrahedron chains, the can almost not activate this mineral. These cations may attach on the site where Al3+ exists on the muscovite surface, just like spodumene, muscovite can not be activated well by such cations. Pt2+ has a large ion radius, as Pauling’s rules depicts polyhedron can not attach to Si tetrahedron well, the adsorption ability of Pt2+ on quartz is low and quartz is activated badly by Pt2+. On the other Pt2+ can adsorb well on spodumene and muscovite well and activated them well because it is not affected so bad by the tetrahedron oxygen anions of the minerals for their its large radius. The isothermal of Ca2+ on quartz indicates a Ca2+ coordinates with less than one surface oxygen anion, this means Ca2+ attaches on quartz mainly by physical adsorption. The adsorption abilities on mineral surface and the interaction abilities with oleate acid radical of the transition metal ions with the same valence are guessed to be determined by their d electron number, the rules should be d1<d2<d3<d4>d5<d6<d7<d8<d9>d10. Hydrogen bond may play an important rule in the activation of the mineral by HF and the interaction of the HF activated silicate mineral with collectors. The general rule is high bond valence and small metal ion radius surface species –Me-O can be activated well by HF with sodium oleate as collector. For example – SiIV-OH is neutral while –SiIV-FH+ and –SiVI-FH+0.33 are positively charged, the positively charged surface species are more likely to connect oleate acid radical via hydrogen bonds.

Jan 1, 2003

By S. V. Petrov

Oxidised ores possess a significant share among raw materials which are treated by traditional plant technology. As usual, the chemical composition of these ores is rather simple. They can be treated by standard cyanidation. In this case, the resulting wastes have an alkaline reaction. Their toxicity (in case of ROM ores treatment) is mainly due to the presence cyanides and thicyanades. The tails are dexotified before disposal. However, chemical reagents used cannot provide a complete removal of toxic matters. In this case, this disposal poses a real problem because these tails contain a significant amount of CN and SCN and their behavior during a long disposal should be studied. A sample with a simple composition taken from cyanidation tails was studied. The sample presents itself the quartz low-grade sulfide gold-bearing ore. Sulfide sulfur content is 0.15 per cent,and heavy metals content is 0.023 per cent. Method of testing is described further. The samples were tested under moderate and subarctic climates based on the difference in temperature, moisture and the degree of oxygen saturation of air. The pH of water extract, which was prepared using distilled water, was also determined besides measuring the concentration of cyanides and thiocyanates. This demonstrates the stability of sulfide-bearing minerals in the disposed tails. The tests time was 820 days. It was found that the alkalinity of the samples tends to lower under oxygen-containing conditions in proportion to temperature increasing. Under conditions without oxygen, the pH lowering is minimal. Mineralogical and chemical properties of the ore material give positive alkaline balance during testing. The solid sample contains enough alkaline agents to compensate dangerous to the environment reactions of sulfides oxidation.pH value maintaining under alkaline conditions witnesses to the possibility of a safe disposal of this tails type. The largest amount of cyanide is removed under acid-containing conditions at positive temperatures. The higher the temperature is, the more intensive destruction is. At the moment, of finishing the tests at 20ºC temperature, the residual concentration of CN- was 0.06-0.10 mg/L, at 4ºC, the residual concentration of CN- was 0.2-0.3 mg/L and at -18ºC was 0.4-0.6 mg/L. Under conditions with the lack of oxygen, cyanides can be removed within the first 200 days. Then, this process fully stops. A stabilized cyanides concentration is 3.0-4.0 mg/L. The presence of sulfides increases the content of cyanides at the initial stage of testing. Then, the concentration of SCN at the temperatures above 0ºC decreases rapidly under oxygen-containing conditions. At the rise of temperature, a narrowing of peak at the curve and an increase of the destruction process are observed. At the end of testing, the concentration of thiocyanates in the moisture of wastes was 0.2-0.3 mg/L at the temperature of 20ºC and 0.5-0.6 mg/L at the temperature of 4ºC, respectively. The concentration of thiocyanates contained in a frozen sample and media which have the lack of oxygen stabilizes at a certain level owing to sulfides and does not practically change further. It was found that detoxification of oxidized cyanidation tailings with a simple composition which were disposed as filtration cakes can be possible. In this case, the concentration of cyanide in the moisture of disposed wastes can have a close value or equal to actual concentration during cyanidation. In order to meet the requirements of high ecological safety standards and successful detoxification process of toxic compounds in the tails under the action of natural factors, the conditions of air aeration with oxygen for the whole volume of tails are required. Keywords: cyanides, thiocyanates, storage, detoxification, flotation cakes

Sep 1, 2012

By Naoki Hiroyoshi, Hajime Miki, Tsuyoshi Hirajima, Masami Tsunekawa

Acidic solutions for chalcopyrite leaching contain cupric, ferrous and ferric ions, and the oxidizing power of the solutions is indicated by a redox potential, determined by the concentration ratio of ferric to ferrous ions. This paper reviews our previous studies on the redox potential dependence of chalcopyrite leaching in sulfuric acid solutions. Leaching and anodic-polarization experiments showed that coexistence of cupric and ferrous ions activate anodic dissolution of chalcopyrite, causing faster copper extraction at the potentials below a certain value (critical potential). The analysis of the AC impedance spectra for chalcopyrite electrode indicated that a high-resistance passive layer grows on the chalcopyrite surface without cupric and/or ferrous ions, and that coexistence of these ions causes a formation of another product layer and inhibits the passive layer growth at low potentials. These results are explained by a reaction model assuming the formation of intermediate Cu2S due to chalcopyrite reduction and the subsequent oxidation of the Cu2S. The critical potential corresponds to the redox potential of the Cu2S formation and the predicted values matched with the experimental results. Catalytic effect of silver ions on chalcopyrite leaching was also discussed based on experimental results and the above model.

Jan 1, 2003